49,XYYYY syndrome

Summary

49,XYYYY syndrome is a developmental defect during embryogenesis^[1]. It draws 103 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #65 of 308).^[2]

Key Facts

• 49,XYYYY syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• 49,XYYYY syndrome's instance of is recorded as class of disease^[4].
• 49,XYYYY syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[5].
• 49,XYYYY syndrome's subclass of is recorded as Y chromosome number anomaly^[6].
• 49,XYYYY syndrome's Commons category is recorded as XYYYY syndrome^[7].
• 49,XYYYY syndrome's Orphanet ID is recorded as 99330^[8].
• 49,XYYYY syndrome's different from is recorded as XYYY syndrome^[9].
• 49,XYYYY syndrome's Google Knowledge Graph ID is recorded as /g/11fmh3vffh^[10].
• 49,XYYYY syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99330^[11].
• 49,XYYYY syndrome's ICD-10-CM is recorded as Q98.8^[12].
• 49,XYYYY syndrome's Mondo ID is recorded as MONDO_0020470^[13].
• 49,XYYYY syndrome's Fandom article ID is recorded as lgbta:XYYYY_Syndrome^[14].
• 49,XYYYY syndrome's Miraheze article ID is recorded as lgbta:XYYYY_Syndrome^[15].

Why It Matters

49,XYYYY syndrome draws 103 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #65 of 308).^[2]